Bimetallic metal–organic frameworks are rationally synthesized as templates and employed for porous carbons with retained morphology, high graphitization degree, hierarchical porosity, high surface ...area, CoNx moiety and uniform N/Co dopant by pyrolysis. The optimized carbon with additional phosphorus dopant exhibits excellent electrocatalytic performance for the oxygen reduction reaction, which is much better than the benchmark Pt/C in alkaline media.
Compared with conventional tumor photothermal therapy (PTT), mild‐temperature PTT brings less damage to normal tissues, but also tumor thermoresistance, introduced by the overexpressed heat shock ...protein (HSP). A high dose of HSP inhibitor during mild‐temperature PTT might lead to toxic side effects. Glucose oxidase (GOx) consumes glucose, leading to adenosine triphosphate supply restriction and consequent HSP inhibition. Therefore, a combinational use of an HSP inhibitor and GOx not only enhances mild‐temperature PTT but also minimizes the toxicity of the inhibitor. However, a GOx and HSP inhibitor‐encapsulating nanostructure, designed for enhancing its mild‐temperature tumor PTT efficiency, has not been reported. Thermosensitive GOx/indocyanine green/gambogic acid (GA) liposomes (GOIGLs) are reported to enhance the efficiency of mild‐temperature PTT of tumors via synergistic inhibition of tumor HSP by the released GA and GOx, together with another enzyme‐enhanced phototherapy effect. In vitro and in vivo results indicate that this strategy of tumor starvation and phototherapy significantly enhances mild‐temperature tumor PTT efficiency. This strategy could inspire people to design more delicate platforms combining mild‐temperature PTT with other therapeutic methods for more efficient cancer treatment.
Thermosensitive liposomes made of DPPC and DSPE‐PEG2000 encapsulating GOx, ICG, and GA are presented. This system is used for synergistic starvation therapy, EEPT, and enhanced mild‐temperature PTT against tumors.
Background and Aims
The study objective was to compare the effectiveness of microwave ablation (MWA) and laparoscopic liver resection (LLR) on solitary 3–5‐cm HCC over time.
Approach and Results
From ...2008 to 2019, 1289 patients from 12 hospitals were enrolled in this retrospective study. Diagnosis of all lesions were based on histopathology. Propensity score matching was used to balance all baseline variables between the two groups in 2008–2019 (n = 335 in each group) and 2014–2019 (n = 257 in each group) cohorts, respectively. For cohort 2008–2019, during a median follow‐up of 35.8 months, there were no differences in overall survival (OS) between MWA and LLR (HR: 0.88, 95% CI 0.65–1.19, p = 0.420), and MWA was inferior to LLR regarding disease‐free survival (DFS) (HR 1.36, 95% CI 1.05–1.75, p = 0.017). For cohort 2014–2019, there was comparable OS (HR 0.85, 95% CI 0.56–1.30, p = 0.460) and approached statistical significance for DFS (HR 1.33, 95% CI 0.98–1.82, p = 0.071) between MWA and LLR. Subgroup analyses showed comparable OS in 3.1–4.0‐cm HCCs (HR 0.88, 95% CI 0.53–1.47, p = 0.630) and 4.1–5.0‐cm HCCs (HR 0.77, 95% CI 0.37–1.60, p = 0.483) between two modalities. For both cohorts, MWA shared comparable major complications (both p > 0.05), shorter hospitalization, and lower cost to LLR (all p < 0.001).
Conclusions
MWA might be a first‐line alternative to LLR for solitary 3–5‐cm HCC in selected patients with technical advances, especially for patients unsuitable for LLR.
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•Six types of Mg-loaded biochars were synthesized for NH4+-N and TP adsorption.•Mg2+ exchange is dominant mechanism for ammonium adsorption on Mg-loaded biochars.•Precipitation and ...electrostatic attraction were the possible TP sorption mechanisms.•Magnesium content and PVtot were predominant factors affecting biochar sorption.•Mg-loaded biochars have a great potential in treatment of waste water.
Herein, biochars from 6 different feedstocks (taro straw, corn straw, cassava straw, Chinese fir straw, banana straw, and Camellia oleifera shell) were produced using magnesium chloride (MgCl2) as a modifier due to their sorption behavior toward NH4+-N and phosphorus in an aqueous solution. The biochar characteristics were evaluated, including pH, pHPZC, biochar magnesium content, and total pore volume (PVtot). The experimental results in terms of the kinetics and equilibrium isotherms showed that the cassava straw and banana straw biochars exhibited the theoretical maximum saturated adsorption capacities of 24.04 mg·g−1 (NH4+-N) and 31.15 mg·g−1 (TP), respectively. Biochar produced from these feedstocks had higher magnesium contents and greater total pore volumes, reflecting the significant contributions from magnesium and steric effects. FTIR, XRD, and SEM/EDS analyses demonstrated that NH4+-N and TP sorption mechanisms predominantly involved surface electrostatic attraction, Mg2+ precipitates and complexation with surface hydroxyl functional groups.
The development of efficient photocathodes is of critical importance for the constructions of promising tandem photo‐electrochemical cells. Most known dye‐sensitized photocathodes are prepared with ...the conventional carboxylic or phosphonic acid anchors and require the presence of other terminal linking groups to connect catalysts; they suffer from high synthetic difficulty and low adsorption stability in aqueous media. Here, a compact bilayer photocathode has been prepared by using a pyrene‐based photosensitizer with multiple terminal pyridine moieties as both the anchoring and linking groups to connect a Co hydrogen‐evolution catalyst to the NiO substrate. The catalyst and dye molecule are assembled in a layer‐by‐layer manner on NiO through the metal‐pyridine coordination. This photocathode exhibits good dye adsorption stability in aqueous media. A stable cathodic photocurrent of 70 μA cm−2 was achieved, with H2 being generated at the photocathode under the visible‐light irradiation. The Faraday efficiency of H2 evolution was estimated to be 9.1 %. Transient absorption spectral studies suggest that the interfacial hole transfer occurs within a few picoseconds. The integration of the organic photosensitizer with pyridine anchoring and linking groups is expected to provide a simple method for the fabrication of stable and efficient photocathodes.
NiO Substrate & Co. A photocathode has been prepared by using a pyrene‐based photosensitizer with multiple terminal pyridine moieties as both the anchoring and linking groups to connect a Co hydrogen‐evolution catalyst to the NiO substrate. This photocathode exhibits good dye adsorption and photochemical stability in aqueous solution and is applied in water reduction into hydrogen under irradiation in photo‐electrochemical cells.
Inorganic cesium lead halide perovskites offer a pathway towards thermally stable photovoltaics. However, moisture‐induced phase degradation restricts the application of hole transport layers (HTLs) ...with hygroscopic dopants. Dopant‐free HTLs fail to realize efficient photovoltaics due to severe electrical loss. Herein, we developed an electrical loss management strategy by manipulating poly(3‐hexylthiophene) with a small molecule, i.e., SMe‐TATPyr. The developed P3HT/SMe‐TATPyr HTL shows a three‐time increase of carrier mobility owing to breaking the long‐range ordering of “edge‐on” P3HT and inducing the formation of “face‐on” clusters, over 50 % decrease of the perovskite surface defect density, and a reduced voltage loss at the perovskite/HTL interface because of favorable energy level alignment. The CsPbI2Br perovskite solar cell demonstrates a record‐high efficiency of 16.93 % for dopant‐free HTL, and superior moisture and thermal stability by maintaining 96 % efficiency at low‐humidity condition (10–25 % R. H.) for 1500 hours and over 95 % efficiency after annealing at 85 °C for 1000 hours.
An electrical loss management strategy by using SMe‐TATPyr molecule manipulating dopant‐free Poly(3‐hexylthiophene) (P3HT) has been developed and employed to fabricate efficient and thermally stable CsPbI2Br solar cells. The P3HT/SMe‐TATPyr presents optimized molecular orientation, favorable energy level alignment and effective defect passivation. Based on P3HT/SMe‐TATPyr HTLs, the fabricated devices yield a record‐high efficiency of 16.93 % for CsPbI2Br solar cells with dopant‐free HTLs.
Medulloblastoma (MB) is the most common malignant brain tumor in childhood. It contains at least four distinct molecular subgroups. The aim of this study is to explore novel diagnostic and potential ...therapeutic markers within each subgroup of MB, in particular within Group 4, the largest subgroup, to facilitate diagnosis together with gene therapy. One hundred and six MB samples were examined. Tumor subtype was evaluated with the NanoString assay. Several novel tumor related genes were shown to have high subgroup sensitivity and specificity, including PDGFRA, FGFR1, and ALK in the WNT group, CCND1 in the SHH group, and α‐synuclein (SNCA) in Group 4. Knockdown and overexpression assays of SNCA revealed the ability of this gene to inhibit tumor invasion and induce apoptosis. Methylation‐specific PCR and pyrosequencing analysis showed that epigenetic mechanisms, rather than DNA hypermethylation, might play the key role in the regulation of SNCA expression in MB tumors. In conclusion, we identify SNCA as a novel diagnostic biomarker for Group 4 MB. Some other subgroup signature genes have also been found as candidate therapeutic targets for this tumor.
Here, we identify for the first time that α‐synuclein (SNCA), the biomarker for Parkinson's disease, as a novel sensitive and specific marker for Group 4 medulloblastoma (MB). In addition, some other subtype‐specific signature genes evaluated here also shed light on clinical usage of molecular subtyping as well as potential gene therapy of MB patients.
A simple and general method is presented herein for the in situ preparations of circularly polarized luminescence (CPL)‐active microcrystals with a large luminescence dissymmetry factor glum, high ...fluorescence quantum efficiency (ΦFL), wide emission color tenability, and well‐ordered morphology. The reactions of pyridine‐containing achiral molecules 1–7 with chiral camphor sulfonic acid ((±)‐CSA) gave crystalline microplates formed by hydrogen bonding interactions between the protonated pyridinium units and the sulfonic anions. The chiral information of CSA are effectively transferred to the microcrystals by hydrogen bonding to afford full‐color CPL from deep‐blue to red with glum in the order of 10−2 and ΦFL up to 80 %. Moreover, organic microcrystals with high‐performance white CPL (ΦFL=46 %; |glum|=0.025) are achieved via the light‐harvesting energy transfer between blue and yellow emitters.
As a result of the efficient hydrogen‐bonding‐mediated chirality transfer and light‐harvesting energy transfer, well‐ordered ionic microcrystals formed between pyridine‐containing achiral molecules and chiral camphor sulfonic acid display full‐color and homogeneously white circularly polarized luminescence (CPL) with ΦFL of up to 80 % and glum in the order of 10−2.
At present, one of the major factors limiting the further improvement of inverted (p‐i‐n) perovskite solar cells (PSCs) is trap‐assisted non‐radiative recombination at the perovskite/electron ...transporting layer (ETL) interface. Surface passivation with organic ammonium salt is a powerful strategy to improve the performance of PSCs. Herein, an effective method by using propylamine hydroiodide (PAI) and 1,3‐diaminopropane dihydroiodide (PDADI) is reported to modify the perovskite/ETL interface. These two ammonium salts do not form new perovskite but directly passivate the defects on the perovskite surface after annealing. The results show that the PDADI‐modified perovskite films possess a lower surface defect density and less non‐radiative recombination as well as improved charge carrier transport. Based on this strategy, the PDADI‐modified p‐i‐n PSCs deliver an impressive efficiency of 25.09% (certified 24.58%) with an open‐circuit voltage of 1.184 V. Furthermore, the unencapsulated PDADI‐modified PSCs also exhibit good storage stability, retaining 91% of initial PCE at 65 °C in a N2 glove box for 1300 h. This strategy provides an efficient route to fabricate highly efficient and stable inverted p‐i‐n structured PSCs.
1,3‐diaminopropane dihydroiodide (PDADI) is introduced to modify the perovskite/electron transporting layer (ETL) interface. Based on this strategy, the PDADI‐modified p‐i‐n perovskite solar cells deliver an impressive efficiency of 25.09% (certified 24.58%) at the laboratory scale (0.071 cm2) with an open‐circuit voltage of 1.184 V.
A readily available small molecular hole‐transporting material (HTM), OMe‐TATPyr, was synthesized and tested in perovskite solar cells (PSCs). OMe‐TATPyr is a two‐dimensional π‐conjugated molecule ...with a pyrene core and four phenyl‐thiophene bridged triarylamine groups. It can be readily synthesized in gram scale with a low lab cost of around US$ 50 g−1. The incorporation of the phenyl‐thiophene units in OMe‐TATPyr are beneficial for not only carrier transportation through improved charge delocalization and intermolecular stacking, but also potential trap passivation via Pb–S interaction as supported by depth‐profiling XPS, photoluminescence, and electrochemical impedance analysis. As a result, an impressive best power conversion efficiency (PCE) of up to 20.6 % and an average PCE of 20.0 % with good stability has been achieved for mixed‐cation PSCs with OMe‐TATPyr with an area of 0.09 cm2. A device with an area of 1.08 cm2 based on OMe‐TATPyr demonstrates a PCE of 17.3 %.
A 2D hole‐transporting material with a pyrene core and four phenyl‐thiophene bridged triarylamine groups, OMe‐TATPyr, was readily synthesized at low cost on a gram scale. A power conversion efficiency (PCE) of up to 20.6 % (average PCE 20.0 %) was achieved for mixed‐cation perovskite solar cells with OMe‐TATPyr, outperforming devices with Spiro‐OMeTAD.
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